돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4587생성일: 2026년 10월 23일

Ethanol → 2-(4-Acetylaminobenzoyloxy)ethyl 2,6-dimethyl-5-methoxycarbonyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate

https://huagongshe.com/ko/reaction/4587

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Methyl 3-aminocrotonateHCID 643918—
반응물2-(4-Acetylaminobenzoyloxy)ethyl 2-(3-nitrobenzylidene)acetylacetateHCID 57265676—
생성물2-(4-Acetylaminobenzoyloxy)ethyl 2,6-dimethyl-5-methoxycarbonyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylateHCID 364874694%

반응 단계

20 g (0.05 moles) of 2-(4-acetylaminobenzoyloxy)ethyl 2-(3-nitrobenzylidene)acetylacetate and 5.23 g (0.05 moles) of methyl 3-aminocrotonate are heated under reflux in 45 ml of ethanol for 8 hours. The solution is then cooled to room temperature to obtain 2-(4-acetylaminobenzoyloxy)ethyl 2,6-dimethyl-5-methoxycarbonyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate as a yellow powder melting at 190°-193° C. The yield is 94% of the theoretical yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727066
출처 데이터셋uspto-grants-1988_02
ORD IDord-7474294ae7e34856979084eb68096e62
출처 메모uspto-grants-1988_02